A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338109



Internal ID20995662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:47326506..47371736hg38UCSC Ensembl
chr2:47553645..47598875hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3845231
hg1945231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3853n223
Supporting Variantsnssv18089396
Samples
Known GenesEPCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338109
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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